Atypical teratoid/rhabdoid tumor metastasizing to the lumbar spinal cord-Reference-Cited by-同舟云学术

Atypical teratoid/rhabdoid tumor metastasizing to the lumbar spinal cord

Published:2017 Issue:6 Volume:56 Page:303-307
ISSN:0387-1193
Container-title:The Journal of the Japanese Society of Clinical Cytology
language:en
Short-container-title:J. Jpn. Soc. Clin. Cytol

Author:

HASHIMOTO Tetsuya¹,KANAMURO Toshiko¹,NONAMI Yuji¹,AIHARA Yasuo²,KAWAMATA Takakazu²,YAMAMOTO Tomoko³⁴,SAWADA Tatsuo³⁴,NAGASHIMA Yoji³

Affiliation:

1. Laboratory of Pathology, Tokyo Women’s Medical University Hospital

2. Department of Neurosurgery, Tokyo Women’s Medical University Hospital

3. Department of Surgical Pathology, Tokyo Women’s Medical University Hospital

4. Department of Pathology, Tokyo Women’s Medical University

Publisher

The Japanese Society of Clinical Cytology

Link

https://www.jstage.jst.go.jp/article/jjscc/56/6/56_303/_pdf

Reference7 articles.

1. 1) Judkins, A. R., Eberhart, C. G., Wesseling, P., Hasselblatt, M. Atypical teratoid/rhabdoid tumor. Louis, D. N., Ohgaki, H., Wiestler, O. D., Cavenee, W. K., eds. WHO Classification of Tumours of the Central Nervous System. Lyon : IARC Press ; pp209-212, 2016.

2. 4) Horiguchi, H., Nakata, S., Nobusawa, S., Uyama, S., Miyamoto, T., Ueta, H. et al. Adult-onset atypical teratoid/rhabdoid tumor featuring long spindle cells with nuclear palisading and perivascular pseudorosettes. Neuropathology 2017 ; 37 : 52-57.

3. 5) DiPatri, A. J. Jr., Sredni, S. T., Grahovac, G., Tomita, T. Atypical teratoid/rhabdoid tumors of the posterior fossa in children. Childs Nerv Syst 2015 ; 31 : 1717-1728.

4. 7) Hasselblatt, M., Gesk, S., Oyen, F., Rossi, S., Viscardi, E., Giangaspero, F. et al. Nonsence mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI-1) expression. Am J Surg Pathol 2011 ; 35 (6) : 933-935.

5. 8) Schneppenheim, R., Fruhwald, M. C., Gesk, S., Hasselblatt, M., Jeibmann, A., Kordes, U., et al. Germline nonsence mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome. Am J Hum Genet 2010 ; 86 (2) : 279-284.